Mohamed Imran

1.6k total citations
26 papers, 130 citations indexed

About

Mohamed Imran is a scholar working on Genetics, Molecular Biology and Infectious Diseases. According to data from OpenAlex, Mohamed Imran has authored 26 papers receiving a total of 130 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 7 papers in Molecular Biology and 5 papers in Infectious Diseases. Recurrent topics in Mohamed Imran's work include Genomics and Rare Diseases (7 papers), SARS-CoV-2 and COVID-19 Research (4 papers) and Pharmacogenetics and Drug Metabolism (4 papers). Mohamed Imran is often cited by papers focused on Genomics and Rare Diseases (7 papers), SARS-CoV-2 and COVID-19 Research (4 papers) and Pharmacogenetics and Drug Metabolism (4 papers). Mohamed Imran collaborates with scholars based in India, United Kingdom and United States. Mohamed Imran's co-authors include Vinod Scaria, Bani Jolly, Mercy Rophina, Sridhar Sivasubbu, Abhinav Jain, Rahul C. Bhoyar, Vigneshwar Senthivel, Mohit Kumar Divakar, Disha Sharma and Kavita Pandhare and has published in prestigious journals such as Nucleic Acids Research, Journal of Clinical Oncology and PLoS ONE.

In The Last Decade

Mohamed Imran

24 papers receiving 127 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Mohamed Imran India 7 52 37 18 18 17 26 130
Mohit Kumar Divakar India 4 31 0.6× 15 0.4× 6 0.3× 10 0.6× 5 0.3× 16 66
Vigneshwar Senthivel India 6 25 0.5× 39 1.1× 22 1.2× 37 2.1× 2 0.1× 14 110
Thao‐Thy Pham Belgium 10 30 0.6× 39 1.1× 26 1.4× 10 0.6× 4 0.2× 14 299
S Natarajan India 9 21 0.4× 39 1.1× 24 1.3× 8 0.4× 39 2.3× 31 332
Wenfang Wu China 9 76 1.5× 86 2.3× 5 0.3× 24 1.3× 4 0.2× 22 279
Isaac Thom Shawa United Kingdom 7 44 0.8× 22 0.6× 38 2.1× 3 0.2× 10 0.6× 19 150
Serap Beldar Canada 5 93 1.8× 74 2.0× 5 0.3× 13 0.7× 4 0.2× 7 192
Ritika Kapoor Singapore 7 11 0.2× 24 0.6× 27 1.5× 7 0.4× 38 2.2× 16 131
Mallika Imwong Thailand 10 12 0.2× 38 1.0× 11 0.6× 16 0.9× 8 0.5× 22 248
Maria Dolci Italy 10 26 0.5× 46 1.2× 4 0.2× 7 0.4× 31 1.8× 27 175

Countries citing papers authored by Mohamed Imran

Since Specialization
Citations

This map shows the geographic impact of Mohamed Imran's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Mohamed Imran with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mohamed Imran more than expected).

Fields of papers citing papers by Mohamed Imran

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mohamed Imran. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Mohamed Imran. The network helps show where Mohamed Imran may publish in the future.

Co-authorship network of co-authors of Mohamed Imran

This figure shows the co-authorship network connecting the top 25 collaborators of Mohamed Imran. A scholar is included among the top collaborators of Mohamed Imran based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Mohamed Imran. Mohamed Imran is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Bhoyar, Rahul C., Mohamed Imran, Vigneshwar Senthivel, et al.. (2025). Understanding the genetic epidemiology of hereditary breast cancer in India using whole genome data from 1029 healthy individuals. Cancer Causes & Control. 36(7). 673–682. 1 indexed citations
2.
Imran, Mohamed, Arvinden VR, Bhaskar Jyoti Saikia, et al.. (2024). Understanding the variant landscape, and genetic epidemiology of Multiple Endocrine Neoplasia in India. Endocrine. 86(3). 1178–1187.
3.
Senthivel, Vigneshwar, Bani Jolly, Arvinden VR, et al.. (2024). Whole genome sequencing of families diagnosed with cardiac channelopathies reveals structural variants missed by whole exome sequencing. Journal of Human Genetics. 69(9). 455–465. 1 indexed citations
4.
Sivadas, Ambily, Bani Jolly, Rahul C. Bhoyar, et al.. (2024). Landscape of pharmacogenetic variants associated with non-insulin antidiabetic drugs in the Indian population. BMJ Open Diabetes Research & Care. 12(2). e003769–e003769. 12 indexed citations
5.
Sivadas, Ambily, Surabhi Rathore, Bani Jolly, et al.. (2024). The genomic landscape of CYP2D6 variation in the Indian population. Pharmacogenomics. 25(3). 147–160. 2 indexed citations
6.
Imran, Mohamed, Rahul C. Bhoyar, Abhinav Jain, et al.. (2023). Genetic epidemiology of monogenic dyslipidemia and statin-associated adverse drug phenotypes in Indian population from whole-genomes of 1029 self-declared healthy individuals. Human Gene. 39. 201252–201252. 2 indexed citations
7.
Divakar, Mohit Kumar, Abhinav Jain, Rahul C. Bhoyar, et al.. (2023). Whole-genome sequencing of 1029 Indian individuals reveals unique and rare structural variants. Journal of Human Genetics. 68(6). 409–417. 2 indexed citations
8.
Kim, Richard H. J., Arjun K. Pathak, Mohamed Imran, et al.. (2023). Nano-compositional imaging of the lanthanum silicide system at THz wavelengths. Optics Express. 32(2). 2356–2356. 3 indexed citations
9.
Imran, Mohamed, et al.. (2023). Magseed® & Magtrace® for the localisation of tumour & sentinel lymph node in breast cancer. European Journal of Surgical Oncology. 49(2). e91–e91.
10.
Rophina, Mercy, Rahul C. Bhoyar, Mohamed Imran, et al.. (2022). Genetic landscape of human neutrophil antigen variants in India from population‐scale genomes. HLA. 101(3). 262–269. 1 indexed citations
11.
Senthivel, Vigneshwar, Rahul C. Bhoyar, Abhinav Jain, et al.. (2022). 1029 genomes of self-declared healthy individuals from India reveal prevalent and clinically relevant cardiac ion channelopathy variants. Human Genomics. 16(1). 30–30. 3 indexed citations
12.
Jha, Pankaj, Disha Sharma, Rahul C. Bhoyar, et al.. (2022). Landscape of Variability in Chemosensory Genes Associated With Dietary Preferences in Indian Population: Analysis of 1029 Indian Genomes. Frontiers in Genetics. 13. 878134–878134. 1 indexed citations
13.
Mishra, Neha, Disha Sharma, Rintu Kutum, et al.. (2022). Comprehensive Assessment of Indian Variations in the Druggable Kinome Landscape Highlights Distinct Insights at the Sequence, Structure and Pharmacogenomic Stratum. Frontiers in Pharmacology. 13. 858345–858345. 1 indexed citations
14.
Rophina, Mercy, et al.. (2021). ESC: a comprehensive resource for SARS-CoV-2 immune escape variants. Nucleic Acids Research. 50(D1). D771–D776. 18 indexed citations
15.
Jain, Abhinav, Rahul C. Bhoyar, Ramya Uppuluri, et al.. (2021). Whole genome sequencing identifies novel structural variant in a large Indian family affected with X-linked agammaglobulinemia. PLoS ONE. 16(7). e0254407–e0254407. 3 indexed citations
16.
Bhoyar, Rahul C., Vigneshwar Senthivel, Bani Jolly, et al.. (2021). An optimized, amplicon-based approach for sequencing of SARS-CoV-2 from patient samples using COVIDSeq assay on Illumina MiSeq sequencing platforms. STAR Protocols. 2(3). 100755–100755. 9 indexed citations
17.
Singh, Urvashi B., Mercy Rophina, Rama Chaudhry, et al.. (2021). Variants of concern responsible for SARS‐CoV‐2 vaccine breakthrough infections from India. Journal of Medical Virology. 94(4). 1696–1700. 17 indexed citations
18.
19.
Yadav, Satya Prakash, Rahul C. Bhoyar, Abhinav Jain, et al.. (2020). Asymptomatic reactivation of SARS-CoV-2 in a child with neuroblastoma characterised by whole genome sequencing. IDCases. 23. e01018–e01018. 8 indexed citations
20.
Bhoyar, Rahul C., Uzma Shamim, Abhinav Jain, et al.. (2020). Genomic analysis of patients in a South Indian Community with autosomal dominant cortical tremor, myoclonus and epilepsy suggests a founder repeat expansion mutation in theSAMD12gene. Brain Communications. 3(1). fcaa214–fcaa214. 5 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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